P-73 Synthetic Studies on Proteasome Inhibitors by Rh-Catalyzed Intramolecular Hydroamidation
スポンサーリンク
概要
- 論文の詳細を見る
- 天然有機化合物討論会の論文
- 2006-07-23
著者
-
Kamisaki Haruhi
Graduate School Of Pharmaceutical Sciences Kyoto Univ. Yoshida Sakyo-ku Kyoto 606-8501 Jpn
-
Takemoto Yoshiji
Graduate School Of Pharmaceutical Sciences Kyoto Univ. Yoshida Sakyo-ku Kyoto 606-8501 Jpn
-
Yasui Yoshizumi
World Premier International Res. Center Advanced Inst. For Materials Res. Tohoku Univ. Aoba Sendai 9
-
Yasui Yoshizumi
Graduate School Of Pharmaceutical Sciences Kyoto University
-
Kobayashi Yusuke
Graduate School of Pharmaceutical Sciences, Kyoto University
-
Yanada Reiko
Graduate School of Pharmaceutical Sciences, Kyoto University
-
Yanada Reiko
Graduate School Of Pharmaceutical Sciences Kyoto University
-
Takemoto Yoshiji
Graduate School Of Pharmaceutical Sciences Kyoto Univ.
-
Yasui Yoshizumi
Graduate School Of Pharmaceutical Sciences Kyoto Univ.
-
Kobayashi Yusuke
Graduate School Of Pharmaceutical Sciences Kyoto University
関連論文
- Synthesis of 3,3-disubstituted oxindoles through Pd-catalyzed intramolecular cyanoamidation
- P-73 Synthetic Studies on Proteasome Inhibitors by Rh-Catalyzed Intramolecular Hydroamidation
- Antiproliferative Activity of Rhinacanthus nasutus (L.) KURZ Extracts and the Active Moiety, Rhinacanthin C(Pharmacology)
- Stereodivergent Synthesis of Chiral 2-Alkenylaziridines : Palladium(0)-Catalyzed 2,3-cis-Selective Aziridination and Base-Mediated 2,3-trans-Selective Aziridination
- Toward General Access to the Aspidosperma-Type Terpenoid Indole Alkaloids : Synthesis of the Key 3,3-Disubstituted Piperidones through Enantioselective Intramolecular Heck-Type Reaction of Chloroformamides
- P-74 Stereoselective Synthesis of 3-Alkylideneoxindoles Using Tandem Carbometallation and Cross-Coupling Reactions
- Development of Chiral Thiourea Catalysts and Its Application to Asymmetric Catalytic Reactions
- Discovery and Application of Asymmetric Reaction by Multi-Functional Thioureas
- Development of Amino Thiourea Catalysts as an Artificial Enzyme : Their Application to Catalytic Enantioselective Reactions
- Synthesis of Indolo[2,3-b]quinolines by Palladium-catalyzed Annulation of Unsaturated Isothioureas
- Regio- and Enantioselective Allylic Substitution with Less Active N- or O-Nucleophiles Catalyzed by Iridium-Complex of Bis(oxazolinyl)pyridine
- Formal (3+3) cycloaddition of silyl enol ethers catalyzed by trifric imide: domino Michael addition-claisen condensation accompanied with isomerization of silyl enol ethers
- Synthesis of 2-Iminoindolines via Samarium Diiodide Mediated Reductive Cyclization of Carbodiimides
- Formal (3+3) Cycloaddition of Silyl Enol Ethers Catalyzed by Trifric Imide: Domino Michael Addition-Claisen Condensation Accompanied with Isomerization of Silyl Enol Ethers